tert-Butyl 5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate

≥95%

Reagent Code: #114536
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CAS Number 1218790-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 377.67 g/mol
Formula C₁₉H₂₅BClNO₄
badge Registry Numbers
MDL Number MFCD15143612
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This chemical is primarily used in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, due to the presence of the boronate ester group, which facilitates the formation of carbon-carbon bonds. This makes it valuable in the development of biologically active compounds, including potential drug candidates. Additionally, its indole core structure is significant in the synthesis of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or antiviral agents. The tert-butyl group provides stability and can be selectively removed or modified in further synthetic steps.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,420.00
inventory 5g
10-20 days ฿29,910.00
inventory 100mg
10-20 days ฿2,727.00
inventory 1g
10-20 days ฿8,000.00
tert-Butyl 5-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
This chemical is primarily used in organic synthesis as a key intermediate in the preparation of complex molecules, particularly in pharmaceutical research. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, due to the presence of the boronate ester group, which facilitates the formation of carbon-carbon bonds. This makes it valuable in the development of biologically active compounds, including potential drug candidates. Additionally, its indole core structure is significant in the synthesis of compounds with potential therapeutic applications, such as anti-inflammatory, anticancer, or antiviral agents. The tert-butyl group provides stability and can be selectively removed or modified in further synthetic steps.
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